Polyethylene glycol-polyvinyl alcohol grafted copolymer: study of the bioavailability after oral administration to rats

Food Chem Toxicol. 2013 Jul:51 Suppl 1:S3-6. doi: 10.1016/j.fct.2012.12.032. Epub 2013 Jan 12.

Abstract

The absorption, urinary excretion, and the biliary excretion of a single oral dose of 10 or 1000 mg/kg bw of (14)C-polyethylene glycol-polyvinyl alcohol (PEG-PVA) grafted copolymer were studied in adult male and female rats. In a balance/excretion experiment, the total excretion of ingested radioactivity was determined over a period of 168 h and residual radioactivity was detected in selected tissues and the carcass. In a biliary excretion experiment, excretion of radioactivity via the bile duct was determined over a period of 48 h after administration of the substance to cannulated rats. Most, if not all, of the radioactivity (>100%) was excreted within 48 h via the feces regardless of sex or dose. Urinary excretion was very limited: 0.45-0.50% of dose at the low dose and 0.22-0.27% of dose at the high dose. At both dose levels, residual radioactivity in the carcass and all organs and tissues after 168 h was ≤ 0.02% of dose. Biliary excretion was 0.01-0.02% of dose. Based on these findings, the bioavailability of PEG-PVA grafted copolymer was determined to be <1% demonstrating that absorption was virtually negligible following a single oral administration to male and female rats.

Keywords: Bioavailability; EFSA; EPA; European Food Safety Authority; Excipient; Film coating polymer; GLP; Good Laboratory Practice; JECFA; Kollicoat® IR; OECD; Oral; PEG; PEG–PVA; PVA; Polyethylene glycol–polyvinyl alcohol grafted copolymer; The Joint (FAO/WHO) Expert Committee on Food Additives; US Environmental Protection Agency; organisation for economic cooperation and development; polyethylene glycol; polyethylene glycol–polyvinyl alcohol; polyvinyl alcohol.

MeSH terms

  • Animals
  • Bile / metabolism
  • Biological Availability*
  • Dose-Response Relationship, Drug
  • Excipients / administration & dosage
  • Excipients / pharmacokinetics*
  • Female
  • Male
  • Polyvinyls / administration & dosage
  • Polyvinyls / pharmacokinetics*
  • Rats

Substances

  • Excipients
  • Kollicoat IR
  • Polyvinyls